EZH2 mutations are frequent and represent an early event in follicular lymphoma

Csaba Bödör(Semmelweis University), Vera Großmann(Johannes Gutenberg University Mainz), N.P. Popov(Queen Mary University of London), Jessica Okosun(Queen Mary University of London), Ciarán Ó’Riain(Queen Mary University of London), King Tan(BC Cancer Agency), Jacek Marzec(Queen Mary University of London), Shamzah Araf(Queen Mary University of London), Jun Wang(Queen Mary University of London), Abigail M. Lee(Queen Mary University of London), Andrew Clear(Queen Mary University of London), Silvia Montoto(Queen Mary University of London), Janet Matthews(Queen Mary University of London), Sameena Iqbal(Queen Mary University of London), Hajnalka Rajnai(Semmelweis University), Andreas Rosenwald(University of Würzburg), German Ott(University of Würzburg), Elı́as Campo(Universitat de Barcelona), Lisa M. Rimsza(University of Arizona), Erlend B. Smeland(Oslo University Hospital), Wing C. Chan(University of Nebraska Medical Center), Rita M. Braziel(Oregon Health & Science University), Louis M. Staudt(National Cancer Institute), George W. Wright(National Cancer Institute), T. Andrew Lister(Queen Mary University of London), Olivier Elemento(Cornell University), Robert K. Hills(Cardiff University), John G. Gribben(Queen Mary University of London), Claude Chelala(Queen Mary University of London), András Matolcsy(Semmelweis University), Alexander Kohlmann(Munich Leukemia Laboratory (Germany)), Torsten Haferlach(Munich Leukemia Laboratory (Germany)), Randy D. Gascoyne(BC Cancer Agency), Jude Fitzgibbon(Queen Mary University of London)
Blood
September 20, 2013
Cited by 322Open Access
Full Text

Abstract

Gain of function mutations in the H3K27 methyltransferase EZH2 represent a promising therapeutic target in germinal center lymphomas. In this study, we assessed the frequency and distribution of EZH2 mutations in a large cohort of patients with follicular lymphoma (FL) (n = 366) and performed a longitudinal analysis of mutation during the disease progression from FL to transformed FL (tFL) (n = 33). Mutations were detected at 3 recurrent mutation hot spots (Y646, A682, and A692) in 27% of FL cases with variant allele frequencies (VAF) ranging from 2% to 61%. By comparing VAF of EZH2 with other mutation targets (CREBBP, MLL2, TNFRSF14, and MEF2B), we were able to distinguish patients harboring clonal EZH2 mutation from rarer cases with subclonal mutations. Overall, the high incidence of EZH2 mutations in FL and their stability during disease progression makes FL an appropriate disease to evaluate EZH2 targeted therapy.


Related Papers

No related papers found

Powered by citation graph analysis